Startseite Cystic echinococcosis in animals and humans of Maharashtra State, India
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Cystic echinococcosis in animals and humans of Maharashtra State, India

  • V.M. Vaidya EMAIL logo , R.J. Zende , A.M. Paturkar , M.L. Gatne , D.G. Dighe , R.N. Waghmare , S.L. Moon , S.S. Bhave , K.G. Bengale und N.V. Nikale
Veröffentlicht/Copyright: 13. April 2018
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Abstract

Echinococcosis/hydatidosis which is a neglected parasitic zoonosis in the developing country like India. The study was conducted during April, 2010 to March, 2017 to determine the prevalence among slaughtered food animals, dogs and human. The samples were collected from the various slaughterhouses situated in different regions of Maharashtra state. A total of 9464 cattle (male), 3661 buffalo, 47189 sheep, 33350 goats and 13579 pigs were scientifically examined during PM inspection at different slaughterhouses. The study revealed that the prevalence of disease in cattle (3.00%) was highest followed by buffalo (2.05%), pig (1.28%), sheep (0.09%) and goat (0.01%), by PM examination. The average estimated economic losses (direct and indirect) due to hydatidosis were Rs. 8,65,83,566 in cattle, Rs. 44,33,93,900 in buffalo, Rs. 7,24,50,615 in sheep, Rs. 1,88,29,359 in goat and Rs. 5,20,49,081 in pigs. Dog faecal samples analyzed and showed the prevalence of echinococcosis as 4.34% (19/438) by sedimentation method and positive samples were confirmed by PCR assay, whereas in high risk human, 11.09% sera samples were found to be positive for echinococcosis. However, based on data collection for seven years, 58 patients were found to be surgically operated for hydatid cyst removal. The results of the present study indicated that cystic echinococcosis/hydatidosis is prevalent in both human and animal population in study areas which attracts serious attention from veterinary and public health authority to reduce economic burden and in designing appropriate strategy for prevention and control of disease.

  1. Conflict of interest: No financial and personal relationship between the authors and other peoples or organisations has inappropriately influenced (bias this work).

Acknowledgement

The authors thank the Indian Council of Agricultural Research, New Delhi, for financial assistance provided under the sponsored project “Outreach Programme on Zoonotic Diseases” for this work.

References

Aarif K., Suhani B., Mathur K.N., Sharma R.L., Makhdoomi D.M., Nazir A., et al. 2015. Retrospective study of hydatidosis in buffaloes slaughtered in Mirha exports private limited in Punjab. Indian Buffalo Bulletin, 34, 231–240Suche in Google Scholar

Abbasi I., Branzburg A., Campos-Ponce M., Hafez S.K.A., Raoul F., Craig P.S., et al. 2003. Copro-diagnosis of E. granulosus infection in dogs by amplification of a newly identified repeated DNA sequence. American Journal of Tropical Medicine and Hygiene, 69, 324–33010.4269/ajtmh.2003.69.324Suche in Google Scholar

Abebe A., Beyene D., Kumsa B. 2014. Cystic echinococcosis in cattle slaughtered at Gondar Elfora export Abattoir, northwest Ethiopia. Journal of Parasitic Diseases, 38, 404–409. 10.1007/s12639-013-0255-zSuche in Google Scholar PubMed PubMed Central

Acosta-Jamett G., Cleaveland S., Bronsvoort B.M., Cunninghamb A.A., Bradshaw H., Craig, P.S. 2010. Echinococcus granulosus infection in domestic dogs in urban and rural areas of the Coquimbo region, North-central Chile. Veterinary Parasitology, 169, 117–122. 10.1016/j.vetpar.2009.12.005Suche in Google Scholar PubMed

Adane M., Guadu, T. 2014. Bovine hydatidosis: occurrence, economic and public health importance in Gondar Elfora abattoir. European Journal of Applied Science, 6, 11–19. 10.5829/idosi.ejas.2014.6.2.8585Suche in Google Scholar

Bekele J., Butako B. 2011. Occurrence and financial loss assessment of cystic echinococcosis (hydatidosis in cattle slaughtered at Wolayita Sodo municipal abattoir, Southern Ethiopia. Tropical Animal Health and Production, 43, 221–228. 10.1007/s11250-010-9680-5Suche in Google Scholar PubMed

Ben-Shimol S., Sagi O., Houri O., Bazarsky E., Berkowitz A., Bulkowstein S., et al. 2016. Cystic echinococcosis in Southern Israel. Acta Parasitologica, 61, 178–186. 10.1515/ap-2016-00Suche in Google Scholar PubMed

Bhattacharya D., Bera A.K., Bera B.C., Maity A., Das S.K. 2007. Genotypic characterization of Indian cattle, buffalo and sheep isolates of Echinococcus granulosus. Veterinary Parasitology, 143, 371–374. 10.1016/j.vetpar.2006.09.007Suche in Google Scholar PubMed

Bijuwork A., Kebede N., Tibat T., Tilahun G., Kassa T. 2013. Occurrences and financial significance of bovine cystic echinococcosis in Southern Wollo, North-eastern Ethiopia. Journal of Veterinary Medicine and Animal Health, 5, 51–56. 10.5897/JVMAH12.072Suche in Google Scholar

Blancas M.M., Herrera E.R., Rodrguez P.C., Tavizn G.J.P., Mercado R.M., Badillo A.V., et al. 2007. Gender as a factor of susceptibility to infection in experimental hydatidosis. Revista Latinoamericana de Microbiologia, 49, 31–37. 10.0000/PMID18693550Suche in Google Scholar PubMed

Borji H., Naghibi A., Jahangiri F. 2012. Copro-DNA test for diagnosis of canine echinococcosis. Comparative Clinical Pathology, 22, 909–912. 10.1007/s00580-012-1498-2Suche in Google Scholar

Craig P.S., Gasser R.B., Parada L., Cabrera P., Parietti S., Borgues C., et al. 1995. Diagnosis of canine echinococcosis: comparison of copro-antigen and serum antibody tests with arecoline purgation in Uruguay. Veterinary Parasitology, 56, 293–30110.1016/0304-4017(94)00680-BSuche in Google Scholar

Daryani A., Alaei R., Arab R., Sharif M., Dehghan M.H., Ziaei H. 2007. The prevalence, intensity and viability of hydatid cysts in slaughtered animals in the Ardabil province of Northwest Iran. Journal of Helminthology, 81, 13–17. 10.1017/S0022149X0720731XSuche in Google Scholar PubMed

Debas E., Ibrahim N. 2013. Prevalence and economic importance of hydatidosis in cattle slaughtered at North Gonder Elfora abattoir. European Journal of Applied Science, 5, 29–35. 10.5829/idosi.ejas.2013.5.1.6564Suche in Google Scholar

Dinkel A., von Nickisch-Rosenegk M., Bilger B., Merli M., Lucius R., Romig T. 1998. Detection of Echinococcus multilocularis in the definitive host: coprodiagnosis by PCR as an alternative to necropsy. Journal of Clinical Microbiology, 36, 1871–187610.1128/JCM.36.7.1871-1876.1998Suche in Google Scholar PubMed PubMed Central

Edo T., Tsegay A.K. 2015. Prevalence of small ruminant hydatidosis and its economic impact at Asella Municipal Abattoir. Food Science and Quality Management, 45, 213–218Suche in Google Scholar

Fagzel F., Ghanbary H. 2002. “Hydatid cyst of the orbit”. Journal of Isfahan Medical School, 20, 65Suche in Google Scholar

Fromsa A., Jobre Y. 2011. Infection prevalence of hydatidosis (E. granulosus, Batsch, 1786) in domestic animals in Ethiopia: A synthesis report of previous surveys. Ethiopian Veterinary Journal, 15, 11–33. 10.4314/evj.v15i2.67691Suche in Google Scholar

Getaw A., Beyena D., Ayana D., Megersa B., Abunna F. 2010. “Hydatidosis: Prevalence and its economic importance in ruminants slaughtered at Adama municipal abattoir, Central Oromia, Ethiopia. Acta Tropica, 113, 221–225. 10.1016/j.actatropica.2009.10.019Suche in Google Scholar PubMed

Godara R., Katoch R., Yadav A. 2014. Hydatidosis in goats in Jammu, India. Journal of Parasitic Diseases, 38, 73–76. 10.1007/s12639-012-0191-3Suche in Google Scholar PubMed PubMed Central

Gudewar J., Pan D., Bera K., Das S.K., Konar A., Rao J.R., et al. 2009. Molecular characterisation of Echinococcus granulosus of Indian animal isolates on the basis of nuclear and mitochondrial genotype. Molecular Biology Reports, 36, 1381–1385. 10.1007/s11033-008-9324-2Suche in Google Scholar PubMed

Gupta N., Javed A., Puri S., Jain S., Singh S., Agarwal A.K. 2011. Hepatic Hydatid: PAIR, Drain or Resrct? Journal of Gastrointestinal Surgery, 15, 1829-36. 10.1007/s11605-011-1649-9Suche in Google Scholar PubMed

Haftu B., Kebede T. 2014. Study on prevalence and economic significance of bovine hydatidosis in Bako municipal abattoir, West Shoa Zone, Oromiya regional state. Journal of Veterinary Science and Technology, 5, 197. 10.4172/2157-7579.1000197Suche in Google Scholar

Heidari Z., Mohebali M., Zarei Z., Aryayipour M., Eshraghian M. R., Kia E. B. et al. 2011. Seroepidemiological study of human hydatidosis in Meshkinshahr District, Ardabil Province, Iran. Iranian Journal of Parasitology, 6, 19–25Suche in Google Scholar PubMed

Ibrahim M.M. 2010. Study of cystic echinococcosis in slaughtered animals in Al Baha region Saudi Arebia: interaction between some biotic and abiotic factors. Acta Tropica, 113, 26–33. 10.1016/j.actatropica.2009.08.029Suche in Google Scholar PubMed

Kayal A. Hussain A. 2014. A comprehensive prospective clinical study of hydatid disease. Hindawi Publishing Corporation ISRN Gastroenterology. Volume 2014, Article ID 514757, p 510.1155/2014/514757Suche in Google Scholar

Latif A.A., Tanveer A., Maqbool A., Siddiqi N., Lyaw-Tanner M., Traub R.J. 2010. Morphological and molecular characterisation of Echinococcus granulosus in livestock and humans in Punjab, Pakistan. Veterinary Parasitology, 170, 44–49. 10.1016/j.vetpar.2010.02.003Suche in Google Scholar PubMed

Melaku A., Lukas B., Bogale B. 2012. Cyst viability, organ distribution and financial losses due to hydatidosis in cattle slaughtered at Dessie Municipal Abattoir, North-eastern Ethiopia. Veterinary World, 5, 213–218. 10.5455/vetworld.2012.213-218Suche in Google Scholar

Ochi E. B., Simplisio E.A., Ismail A.O. 2015. A retrospective study on the major causes of meat condemnations in animals slaughtered in Juba county, South Sudan. International Journal of Bioassays, 4, 4620–4624. https://doi.org/10.21746/ijbio.2015.12.008Suche in Google Scholar

OIE. 2008. Echinococcosis/hydatidosis. Chapter 2.1.4. In: OIE Terrestrial Manual. pp.175-190.Suche in Google Scholar

Pednekar R.P., Gatne M.L., Andrew Thompson R.C., Traub R.J. 2009. Molecular and morphological charecterization of Echinococcus from food producing animals in India. Veterinary Parasitology, 165, 58–65. 10.1016/j.vetpar.2009.06.021Suche in Google Scholar

Pour A.A., Hosseini S.H., Shayan P. 2012. The prevalence and fertility of hydatid cysts in buffaloes from Iran. Journal of Helminthology, 86, 373–377. 10.1017/S0022149X11000514Suche in Google Scholar PubMed

Prathiush P.R., D’Souza P.E., Gowda A.K.J. 2008. Diagnosis of Echinococcus granulosus infection in dogs by a coproantigen sandwich ELISA. Veterinarski Arhiv, 78, 297–305.Suche in Google Scholar

Rahimi M.T., Sharifdini M., Ahmadi A., Laktarashi B., Mahdavi S.A., Kia E.B. 2011. Hydatidosis in human and slaughtered herbivores in Mazandaran province, northern Iran. Asian Pacific Journal Tropical Diseases, 1, 212–215. 10.1016/S2222-1808(11)60031-5Suche in Google Scholar

Regassa A., Abunna F., Mulugeta A., Megersa B. 2009. Major metacestodes in cattle slaughtered at Wolayita Sodo municipal abattoir, Southern Ethiopia: Prevalence, cyst viability, organ distribution and socioeconomic implications. Tropical Animal Health and Production, 41, 1495–1502. 10.1007/s11250-009-9338-3Suche in Google Scholar PubMed

Robinson M.W., Dalton J.P. 2009. Zoonotic helminth infections with particular emphasis on fasciolosis and other trematodiases. Philosophical Transactions of the Royal Society B: Biological Sciences, 364, 2763–2776. 10.1098/rstb.2009.0089Suche in Google Scholar PubMed PubMed Central

Sajjan S.A., Paturkar A.M., Zende R.J., Vaidya V.M., Chethan Kumar H.B. 2015. Prevalence of hydatidosis in domestic pigs and elucidation of its economic impact on pork production. Indian Veterinary Journal, 92, 15–18Suche in Google Scholar

Sangaran A., Arunkumar S., John Lalitha. 2014. Incidence of hydatidosis in slaughtered sheep and goat. Indian Journal of Veterinary and Animal Science, 43, 156–158Suche in Google Scholar

Sariozkan S., Yalcin C. 2009. Estimating the production losses due to cystic echinococcosis in ruminants in Turkey. Veterinary Parasitology, 163, 330–334. 10.1016/j.vetpar.2009.04.032Suche in Google Scholar PubMed

Shahnazi M., Jafari A., Javadi M., Saraei M. 2013. Fertility of hydatid cysts and viability of protoscoleces in slaughtered animals in Qazvin, Iran. Journal of Agricultural Science, 5, 141–146. http://dx.doi.org/10.5539/jas.v5n1p14110.5539/jas.v5n1p141Suche in Google Scholar

Shaikenov B.S., Rysmukhambetova A.T., Massenov B., Deplazes P., Mathis A., Torgerson, P.R. 2004. The use of a polymerase chain reaction to detect Echinococcus granulosus (G1 strain) eggs in soil samples. American Journal of Tropical Medicine and Hygiene, 71, 441–443. https://doi.org/10.4269/agtmh.2004.71.44110.4269/ajtmh.2004.71.441Suche in Google Scholar

Shambesh M.A., Craig P., Macpherson C.N., Rogan M.T., Gusbi A.M., Echtuish E.F. 1999. An extensive ultrasound and serologic study to investigate the prevalence of human cystic echinococcosis in northern Libya. American Journal of Tropical Medicine and Hygiene, 60, 462–46810.4269/ajtmh.1999.60.462Suche in Google Scholar PubMed

Singh B.B., Singh G., Sharma R., Sharma J.K., Aulakh R.S., Gill, J.P.S. 2013. Human hydatidosis: an under discussed occupational zoonosis in India. Helminthologia, 50, 87–90. 10.2478/s11687-013-0113-7Suche in Google Scholar

Singh B.B., Sharma J.K., Tuli A., Sharma R., Bal M.S., Aulakh R.S. et al. 2014. Prevalence and morphological characterization of Echinococcus granulosus from Maharashtra. Journal of Parasitic Diseases, 38, 36–40. 10.1007/s12639-012-0189-xSuche in Google Scholar PubMed PubMed Central

Stefanic S., Shaikenov B.S., Deplazes P., Dinkel A., Torgerson P.R., Mathis, A. 2004 Polymerase chain reaction for detection of patent infections of Echinococcus granulosus (“sheep strain”) in naturally infected dogs. Parasitology Research, 92, 347–351. 10.1007/s00436-003-1043-ySuche in Google Scholar PubMed

Thrusfield, M. 2005. Veterinary epidemiology, 3rd edition. United Kingdom. Blackwell Sciences Ltd. 626Suche in Google Scholar

Tilahun A., Terefe Y. 2013. Hydatidosis: prevalence, cyst distribution and economic significance in cattle slaughtered at Arbaminch municipality abattoir, Southern Ethiopia. Global Veterinaria, 11, 329–334. 10.5829/idosi.gv.2013.11.3.2300Suche in Google Scholar

Wang Q., Huang Y., Huang L., Yu W., He W., Zhong B. et al. 2014. Review of risk factors for human echinococcosis prevalence on the Qinghai-Tibet Plateau, China: a prospective for control options. Infectious Diseases of Poverty, 3, 3. 10.1186/2049-9957-3-3Suche in Google Scholar PubMed PubMed Central

WHO 2002. WHO/OIE Manual on Echinococcosis in humans and animals: a public health problem of global concern, Eckert J., Gemmell, M.A., Meslin F.X., Pawlowski Z.S., (eds.) OIE (World Organisation for Animal Health, Paris, France, 1-262Suche in Google Scholar

WHO 2009. Analysis of the economic impact of cystic echinococcosis in Spain. Benner C., Carabin H., SánchezSerrano L., Budke C., Carmena D. Bulletin of the World Health Organization, 88, 4957. 10.2471/BLT.09.066795Suche in Google Scholar PubMed PubMed Central

WHO 2017. Echinococcosis. Fact sheet No. 377. http://www.who.int/mediacentre/factsheets/fs377/en/ updated March 2017Suche in Google Scholar

Received: 2017-7-20
Revised: 2017-11-30
Accepted: 2017-12-11
Published Online: 2018-4-13
Published in Print: 2018-6-26

© 2018 W. Stefański Institute of Parasitology, PAS

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